Quercetin alleviates myocyte toxic and sensitizes anti-leukemic effect of adriamycin

被引:18
|
作者
Han, Yanqiu [1 ,2 ]
Yu, Hong [2 ]
Wang, Junrui [1 ]
Ren, Yanzhen [2 ]
Su, Xiulan [1 ,3 ]
Shi, Yingxu [1 ]
机构
[1] Inner Mongolia Med Univ, Affiliated Hosp, Clin Lab, 1 Tongdao North St, Hohhot 010050, Peoples R China
[2] Inner Mongolia Med Univ, Affiliated Hosp, Dept Hematol, Hohhot 010050, Peoples R China
[3] Inner Mongolia Med Univ, Affiliated Hosp, Clin Res Ctr, Hohhot 010050, Peoples R China
基金
中国国家自然科学基金;
关键词
Leukemia; Xenograft nude mice; Quercetin; Adriamycin; Myocyte damage; CANCER-RISK; FLAVONOIDS; DOXORUBICIN; ACTIVATION; RECEPTOR; PROTEIN; CELLS; MECHANISMS; TUMOR; BCL-2;
D O I
10.1179/1607845414Y.0000000198
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Derived from plants, flavonoids have been proven to possess anti-cancer activities. Adriamycin (ADM), an anthracycline antibiotic, is widely applied in the chemotherapy for leukemia; however, it has a side effect of heart damage. This study aims to explore potential anti-leukemia effects of quercetin (Que) and the underlying mechanism. Methods: The P388 xenograft mice models were first established and then treated with Que alone or in combination with ADM. Subsequently, we evaluated their effects on cell proliferation and apoptosis by observing the cell cycle and detecting the Caspase-3 level, respectively. The underlying pro-apoptotic mechanism was further investigated by detecting the expression levels of NF-kappa B, Bcl-2, and Bax. The cardiomyocyte ultrastructural changes of P388 leukemic mice after drug treatment were also observed. The protective effect of Que on cardiomyocyte was evaluated by detecting enzymatic activity changes of glutathione peroxidase, superoxide dismutase, and malondialdehyde. Results: Compared with ADM group, the combination of ADM and Que showed prolonged survival time and less peripheral white blood cells. Que could sensitize the anti-leukemic effect of ADM by inhibiting the proliferation of white blood cells through trapping the cells at the S phase; caspase-3 was activated via the expressional regulation of Bcl-2, Bax, and NF-kappa B. When applied in combination with ADM, Que could attenuate heart damage by cleaning the reactive oxygen species. Conclusion: Our study may provide informative evidences for the underlying mechanism of anti-cancer effects of Que and sheds light on the clinical application of Que in leukemia treatment.
引用
收藏
页码:276 / 283
页数:8
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